Sudden neonatal death in carnitine transporter deficiency
Open Access
- 1 August 1997
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 131 (2), 304-305
- https://doi.org/10.1016/s0022-3476(97)70171-9
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporterClinical Cardiology, 1996
- Inborn errors of metabolism diagnosed in sudden death cases by acylcarnitine analysis of postmortem bileClinical Chemistry, 1995
- Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liverHuman Pathology, 1994
- Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptakeAnnals of Neurology, 1991
- Primary Carnitine Deficiency Due to a Failure of Carnitine Transport in Kidney, Muscle, and FibroblastsNew England Journal of Medicine, 1988
- Role of carnitine during developmentCanadian Journal of Physiology and Pharmacology, 1985